Orange Book product · Generic (ANDA)
HYDROCORTISONE ACETATE 1% AND PRAMOXINE HYDROCHLORIDE 1%
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
At a glance
May 17, 1988
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 17, 1988
38 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Strength
1%;1%
Dosage form
AEROSOL, METERED
Route
TOPICAL
TE code
Not listed
Application
ANDA 089440
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
- —EPIFOAMGeneric (ANDA)
ANDA 086457 · MYLAN SPECIALITY LP
- —PROCTOFOAM HCGeneric (ANDA)
ANDA 086195 · MYLAN SPECIALITY LP
- —PRAMOSONEGeneric (ANDA)
ANDA 083778 · LEGACY PHARMA
- —PRAMOSONEGeneric (ANDA)
ANDA 085368 · LEGACY PHARMA
- —PRAMOSONEGeneric (ANDA)
ANDA 083213 · FERNDALE LABS
- —PRAMOSONEGeneric (ANDA)
ANDA 085980 · LEGACY PHARMA
- —PRAMOSONEGeneric (ANDA)
ANDA 085979 · LEGACY PHARMA
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
